Antifungal, antiaflatoxigenic, and cytotoxic properties of bioactive secondary metabolites derived from Bacillus species

Aflatoxins (AFs) are hazardous carcinogens and mutagens produced by some molds, particularly Aspergillus spp. Therefore, the purpose of this study was to isolate and identify endophytic bacteria, extract and characterize their bioactive metabolites, and evaluate their antifungal, antiaflatoxigenic, and cytotoxic efficacy against brine shrimp (Artemia salina) and hepatocellular carcinoma (HepG2). Among the 36 bacterial strains isolated, ten bacterial isolates showed high antifungal activity, and thus were identified using biochemical parameters and MALDI-TOF MS. Bioactive metabolites were extracted from two bacterial isolates, and studied for their antifungal activity. The bioactive metabolites (No. 4, and 5) extracted from Bacillus cereus DSM 31T DSM, exhibited strong antifungal capabilities, and generated volatile organic compounds (VOCs) and polyphenols. The major VOCs were butanoic acid, 2-methyl, and 9,12-Octadecadienoic acid (Z,Z) in extracts No. 4, and 5 respectively. Cinnamic acid and 3,4-dihydroxybenzoic acid were the most abundant phenolic acids in extracts No. 4, and 5 respectively. These bioactive metabolites had antifungal efficiency against A. flavus and caused morphological alterations in fungal conidiophores and conidiospores. Data also indicated that both extracts No. 4, and 5 reduced AFB1 production by 99.98%. On assessing the toxicity of bioactive metabolites on A. salina the IC50 recorded 275 and 300 µg/mL, for extracts No. 4, and 5 respectively. Meanwhile, the effect of these extracts on HepG2 revealed that the IC50 of extract No. 5 recorded 79.4 µg/mL, whereas No. 4 showed no cytotoxic activity. It could be concluded that bioactive metabolites derived from Bacillus species showed antifungal and anti-aflatoxigenic activities, indicating their potential use in food safety.


Antifungal activity of bioactive metabolites
The six extracts of the two bacterial isolates, Bacillus cereus (No.RQ13) and Bacillus thuringiensis (No.RQ22) were used to investigate the antifungal activity against different fungal species (

Polyphenols in bioactive metabolites
The ability of the two extracts No. 4 and 5 to produce polyphenols was investigated.Nine phenolic acids were detected (Table 6, Figure S7) in extract No. 4, whereas cinnamic acid and syringic acid were the most abundant phenolic acids at concentrations of 19.57 and 15.18 µg/g, respectively.Extract No. 4 reflected a distinguished content of flavonoids, with the detection of three compounds (Table 6).Daidzein and naringenin were detected at 24.10 and 14.38 µg/g, respectively.On the other hand, rutin was detected in relatively low concentrations recording 0.01 µg/g.Nine phenolic acids have been detected (Table 6, Figure S8) in extract No. 5, whereas 3, 4-dihydroxybenzoic acid was the most abundant phenolic acid at a concentration of 560.22 µg/g.Cinnamic acid and coumaric acid were also detected at high concentrations recording 57.33 and 50.92 µg/g, respectively.A distinguished content of flavonoids was also detected in extract No. 5, with three compounds (Table 6), whereas naringenin was detected at a concentration of 9.22 µg/g.On the other hand, daidzein and rutin were detected at lower concentrations recording 1.60 and 0.02 µg/g, respectively.The effect of extracts No. 4 and 5 on A. flavus structure was determined using a SEM. Figure 3A shows typical conidia and conidiospores of untreated A. flavus.The effect of extract No. 4 on A. flavus spores followed with less deformation but also caused the loss of some fungal spores (Fig. 3B).On the other hand, extract No. 5 had a similar effect on the conidiophores and conidiospores of A. flavus (Fig. 3C).

Antifungal and antiaflatoxigenic activity of bioactive metabolites
The effect of different concentrations of extracts No. 4 and 5 on the fungal growth of A. flavus after 10 days of incubation was studied (Table 7).Results revealed that extracts No. 4 and 5 at 9 mg/mL concentrations reduced fungal growth by 57.32% and 35.98%, respectively.On the other hand, data indicated that different concentrations of extract No. 4 showed variable degrees of antifungal activity, whereas extract No. 5 at concentrations 1 and 3 mg/mL stimulated fungal growth.Inhibition of fungal growth occurred by 21.70%, 30.66%, and 35.98% at concentrations 5, 7, and 9 mg/mL, respectively.It was also noticed that the inhibition of fungal growth increased by increasing the concentration of extracts.The effect of different concentrations of extracts No. 4 and 5 on aflatoxin production was investigated (Table 7).The data indicated that extract No. 4 at a 1 mg/mL concentration, reduced AFB 1, AFB 2 , and AFG 2 by 99.53%, 99.68%, and 100%, respectively.At concentrations of 7 and 9 mg/mL AFB 2 production was completely prevented.On the other hand, AFG 1 production was completely prevented at concentrations 1, 3, 5, 7, and 9 mg/mL.Results also revealed that at a concentration of 9 mg/mL, an increase in AFG 2 production was observed.
In studying the effect of extract No. 5 on aflatoxin production, results indicated that AFB 1 was reduced by 83.41% at a concentration of 1 mg/mL, and AFB 1 production was continuously reduced by increasing the concentration of the extract.For AFB 2 production, the extract at a concentration of 1 mg/mL reduced AFB 2 by 90.73%, whereas at concentrations 7 and 9 mg/mL, AFB 2 was not detected.Data also showed that the extract, at a concentration of 1 mg/mL, reduced AFG 1 by 83.90%, and the reduction increased by increasing the extract concentration to 9 mg/mL to reach 95.70%.On the other hand, AFG 2 was reduced by 70.92% at a concentration of 1 mg/mL, whereas the reduction increased by increasing the concentration to 9 mg/mL to reach 100%.

Brine shrimp lethality bioassay
The effect of extracts No. 4 and 5 on the mortality percentage values of the A. salina are presented in Fig. 4. The toxicity test results revealed the highest percentage of mortality for larvae, which was recorded at a concentration of 600 µg/mL for extract No. 5. On the other hand, extract No. 4 showed the lowest percentage of mortality for larvae, which was recorded at a concentration of 1000 µg/mL.The LC 50 value was obtained based on the mortality of A. salina larvae induced by the extracts, with extract No. 5 showing the highest LC 50 at 300 µg/mL, followed by extract No. 4 at 275 µg/mL.

Cytotoxicity of human cell line
Extract No. 4 showed no anticancer activity; nevertheless, extract No. 5 produced cell toxicity in a concentrationdependent manner (Fig. 5).The IC 50 values were used to express anti-proliferative activity, whereas lower IC 50 values indicated more significant cell growth-inhibiting activity.Data showed that extract No. 5 had an IC 50 value of 79.4 µg/mL, whereas doxorubicin, which was used as a positive control, had an IC 50 value of 21.6 µg/ mL (Figure S9).It was observed that the extracts tested were not active as doxorubicin.

Discussion
One of the most vital points of this research is the screening of novel microorganisms for antifungal activity.The CFS of thirty-six bacterial isolates were tested for their antifungal activity in this study, whereas the CFS of the following bacterial isolates No. RQ2, RQ7, RQ13, RQ15, and RQ22, were the most promising inhibiting Fusarium spp. to a varying degree.Similarly, several authors established the ability of Bacillus strains to successfully biocontrol Fusarium strains [32][33][34] .In another study, eight newly grown Bacillus isolates (GB31, GB41X, XJ11, XG11, B. sub2, XJ2, XJ8, and XI4) effectively inhibited the growth of more than two F. graminearum strains in vitro 35 .
Aspergillus flavus is a microscopic saprophyte fungus that is both pathogenic and toxic and is common in nature and reduces the quality and safety of raw materials and products.The CFS of the bacterial isolates No.   37 reported that the antifungal activity of the B. subtilis CW14 supernatants was the best, inhibiting mycelial growth and spore germination of A. ochraceus.The antifungal activity of Bacillus isolates could be attributed to the generation of antifungal chemicals that influence the morphological development of fungal structures, such as hyphae growth, morphology, and spore germination 15 .
The bacterial isolates showing high antifungal activity were identified using biochemical parameters and MALDI-TOF MS analysis.The MALDI-TOF MS has been used as a quick, high-throughput bacterial identification technology in diagnostic microbiology laboratories 38 .However, this identification technique's efficacy depends on the reference strains obtained in the mass spectral database 39 .As previously stated, spectral analysis with MALDI-TOF MS can complete identifications as high as 16S rRNA sequences due to its ability to identify at the species level 40,41 .
The bacterial isolates No. RQ13 and RQ22 which showed higher antifungal activity were thus selected to extract and characterize their bioactive secondary metabolites, whereas VOCs were identified using gas chromatography-mass spectrometry (GC/MS).Our results revealed twelve VOCs were detected in extract No. 4, whereas seven VOCs were detected in extract No.5.Our results were considered lower than those reported by Gao et al. 42 , who isolated and identified B. subtilis CF-3, and later found that during the fermentation process, a  45 .Furthermore, the results agree with Zhang et al. 46 , who showed that B. subtilis might produce antibiotics, antifungal proteins, and a variety of VOCs 47 .
The main components in extract No. 4 were butanoic acid, 2-methyl (37.64%), and iso-valeric acid (21.62%).On the contrary, Sadiq and Jamil 48 revealed that the extract of intracellular compounds produced by B. cereus showed the presence of VOCs such as toluene, acetic acid butyl ester, 2-Pentanol acetate, and propanoic acid.The VOC hexadecanoic acid was also detected at low concentrations.Similar observations were reported by Rajaofera et al. 44 , who noted that hexadecanoic acid is one of the compounds produced by B. atrophaeus strain HAB-5.The most critical components identified in extract No. 5, were 9, 12-Octadecadienoic acid (Z,Z)-(81.29%),and hexadecanoic acid (7.75%).Similar results were reported by Jangir et al. 49 , who identified the following compounds; namely 9,12-octadecadienoic acid (Z,Z)-, and hexadecanoic acid from B. subtilis.
One of the most significant antifungal compounds detected at a high percentage in extract No. 4 was butanoic acid 2-methyl- 50 .Similar observations were reported by Xu et al. 51 , who stated that VOCs 2 methylbutanoic acid and iso-valeric acid released by B. tequilensis XK29 inhibited the growth of Ceratocystis fimbriata.On the other hand, the VOC 9, 12-octadecadienoic acid (Z,Z) detected at a high percentage in extract No. 5 was confirmed to be an excellent antifungal agent 52 .
Polyphenols are the most abundant type of natural antioxidant, flavonoids, hydrolyzable and condensed tannins, phenolic acids, stilbenes, lignans, and phenolic aldehydes 53 .The LC/MS detected nine phenolic acids in extract No. 4, whereas cinnamic and syringic acids were the most abundant.Extract No. 4 reflected a distinguished content of flavonoids, with the detection of daidzein, naringenin, and rutin.In agreement, Hassan et al. 54 found syringic acid, among other phenolic acids.produced by several Bacillus spp., whereas rutin was the only flavonoid produced.
Nine phenolic acids in extract No. 5 were detected.The phenolic acids 3, 4-dihydroxybenzoic acid, and cinnamic acid were the most abundant.On the other hand, a distinguished content of flavonoids was also detected in extract No. 5, with the detection of naringenin, daidzein, and rutin.Similar observations were reported by Zhao et al. 55 , who successfully applied to an in vitro study in which catechin/epicatechin-broth samples were anaerobically fermented with gut microbes obtained from healthy human donors, and all bacteria used demonstrated outstanding ability in metabolizing grape polyphenols, whereas 3, 4-dihydroxybenzoic acid was detected among other phenolic acids.
Recently, phenolic compounds have garnered much attention due to their antioxidant activity; additionally, these compounds have been reported to be potential candidates in lowering cardiovascular diseases 56 and anticarcinogenic activities, antiallergenic, anti-atherogenic, anti-inflammatory, antimicrobial, and antithrombotic effects 57 .Phenolics are gaining popularity in the food sector because they slow the oxidative breakdown of lipids, improving food quality and nutritional content 58,59 .
In the setting of developing antibiotic resistance, there is a need for active chemicals that inhibit disease propagation, infection, and virulence.The food production industry also relies heavily on developing novel food preservatives that are less damaging to human and environmental health.This prospective sector of microbial VOC application has yet to be investigated 60 .
Results showed that extracts No. 4 and 5 extracted from B. cereus showed higher antifungal activity against various fungal species.Hathout et al. 61  Later, different concentrations of extract No. 4 and 5 were studied on A. flavus fungal growth, and aflatoxin production after 10 days of incubation.Data showed extracts No. 4 and 5 reduced fungal growth.It was also noticed that increasing the concentration of extracts increased the inhibition of fungal growth.Similar results were reported by Siahmoshteh et al. 15 , who revealed that culture filtrates of soil strains of B. subtilis and B. amyloliquefaciens showed antifungal activity against A. parasiticus NRRL2999.In agreement, Khan et al. 34 reported that 100 µg/mL of 1-butanol extract of d B. subtilis 30VD-1 cell-free culture filtrate caused about 40% inhibition of Fusarium spp.The antifungal activity of extracts No. 4 and 5 might be due to bioactive secondary metabolites such as VOCs and polyphenols, known as antimicrobial compounds.
Data also showed that extracts No. 4 and 5 at a 9 mg/mL concentration reduced AFB 1 production by 99.99% and 99.97%, respectively.On the other hand, extract No. 4 at a concentration of 9 mg/mL completely prevented AFG 1 and reduced AFG 2 output by 99.01%, whereas extract No.5 reduced AFG 1 by 89.76% and prevented AFG 2 production.In experimental animals, Abdel-Wahhab et al. 64 revealed that Bacillus extract at the tested doses improved all biochemical parameters and the histological image in rats that received AFB 1 .In vitro, Pereyra et al. 65 indicated that Bacillus spp.reduced AFB 1 production by A. parasiticus, whereas extracellular metabolites extracted from the Bacillus species inhibited AFB 1 production to non-detectable levels.In another study, the CFS of B. licheniformis CFR1 was able to degrade AFB 1 more efficiently than the cell lysate 66 .Recently, L. rhamnosus bioactive secondary metabolites at a 9 mg/mL concentration reduced AFB 1 production by 99.98% 30 .
The brine shrimp lethality bioassay was initially employed as a simple test to determine toxicity; nevertheless, it is not a specific test.The brine shrimp lethality bioassay is a quick, inexpensive, and straightforward method for assessing the biological activities of extracts and is considered an initial screening method used to evaluate bioactive compounds or compounds assumed suitable as anticancer drugs.The brine shrimp lethality bioassay has been widely used as a preliminary screening of bioactive metabolites to assess their toxicity to A. salina, which could potentially indicate the potential cytotoxic qualities of the test materials 67 .Extract No. 5 showed the highest LC 50, recording 300 µg/mL, followed by extract No. 4, recording an LC 50 of 275 µg/mL.
The current investigation revealed that the degree of mortality of A. salina larvae was proportional to the concentration of the extracts.That could be because the higher the concentration, the more potent bioactive contents can be produced.As there is a correlation between cytotoxicity and activity against A. salina nauplii, the cytotoxic effects of the extracts were chosen for subsequent cell line assay 68 .The extracts showing toxicity against A. salina were studied against HepG2.Results revealed that extract No. 4, which displayed low toxicity against A. salina, showed no anticancer activity.On the other hand, extract No. 5, which showed high toxicity against A. salina, was effective against HepG2 cells by 64.3% at a concentration of 100 µg/mL and recorded an IC 50 of 79.4 µg/mL.Similar results were reported by Haneen et al. 69 , who studied the effect of B. cereus and B. subtilis extracts against human breast adenocarcinoma (MCF-7) and found that at a concentration of 100 µg/mL, the extracts were effective against MCF-7 cells for both B. cereus (48.8%) and B. subtilis (63.8%).In agreement, Ganguly et al. 70 stated that the MTT experiment demonstrated significant cytotoxic activity against MCF-7 with an IC 50 value of 46.64 µg/mL.
This study indicated that bioactive metabolites derived from Bacillus cereus dramatically inhibited AFs production showing a high potential for managing AFs contamination in the food and feed industries.Cytotoxicity experiments using the brine shrimp lethality assay and the HepG2 cell line revealed that Bacillus cereus bioactive metabolites had tolerable toxicity levels, thus indicating that the bioactive metabolites are safe to use in applications involving human or animal food items.
The various biological activities of bacterial bioactive metabolites make them useful in a variety of industrial applications, as they could be utilized to manufacture antibiotics, antifungals, anticancer agents, and antivirals 71 .Bacterial bioactive metabolites could be used in wastewater treatment to eliminate contaminants 72 .They are also essential in the production of bio-fertilizers, biofuels, cosmetics, and biopolymers 72 .Bacterial bioactive metabolites could have considerable therapeutic potential because they include antibacterial, antifungal, antiviral, and antioxidant properties, which are vital in the face of growing drug-resistant microbial infections 71 .

Sampling
Rice grains (1 kg) were gathered from retail stores in Egypt's Qalyubia governorate, and they were transported to the Food Toxicology and Contaminants lab and kept in polythene bags refrigerated (< 10 °C) until examination.

Microorganisms
The genome sequence of the aflatoxin-producing Aspergillus flavus utilized in this work was submitted to the GenBank database as A. flavus AAM2020 (Accession No. OP942201) and was isolated from Egyptian maize samples 73 .From several grains in Egypt, the fungi A. parasiticus, A. niger, A. ochraceus, Fusarium oxysporum, Fusarium spp., and Penicillium spp.were isolated 74 .

Isolation of endophytic bacteria
The rice grains were washed in running water for ten minutes and then washed two times with sterile distilled water for one minute; after that, they were immersed in 3% (v/v) sodium hypochlorite and 70% (v/v) ethanol for three minutes.The rice was washed thrice with sterilized distilled water for two minutes to finish cleaning.Sterilized rice grains were placed on sterilized filter paper before implanted on nutrient agar Petri dishes and incubated at 30 °C for 2 to 7 days 75 .Sub-culturing was employed to select and purify morphologically distinct colonies.Pure cultures were used to evaluate their antifungal activity.

Antifungal activity of CFS of bacterial isolates
Endophytic bacterial isolates were tested for their antifungal activity using the agar well diffusion technique 76 .Isolated endophytic bacteria strains were cultured on tryptic soy broth for 24 h at 37 °C.Following incubation, the broth media were centrifuged (Thermo Fisher Scientific, USA) at 10,000 rpm for 10 min at 4 °C to collect the CFS, which was then filtered using a 0.2 mm sterile Millipore filter (Millex-GS, Millipore, USA).On Petri dishes, potato dextrose agar media was placed, and different fungal isolates (50 µL, 10 6 spores/mL) were dispersed completely over the agar surface with a sterile cotton swab.Wells were cut with a sterile cork borer and each well-received 100 µL of CFS of bacterial isolates.The Petri dishes were incubated for 48 h at 28 °C, and the inhibition zones (mm) were measured to assess the antifungal activity.Biochemical analysis and MALDI-TOF were used to identify endophytic bacterial isolates with antifungal activity.

Identification of bacterial isolates
The bacterial isolates showing antifungal activity were identified using biochemical parameters (Gram staining 77 and oxidase test 78 ) and MALDI-TOF MS.In brief, a loop of freshly bacterial cultures was placed in 300 µL of water and 900 µL of ethanol.The pellets were mixed with equivalent formic acid (70%) and acetonitrile (100%) after centrifugation for 2 min at 13,000 rpm.Using the MALDI-TOF MS technology, the supernatant (extracted bacterial proteins) was utilized for protein identification and profiling (Microflex LT, Bruker, Billerica, MA 01821, USA) 79 .
For identification, the sample (1 µL) was placed on a MALDI bio target plate and left to dry at room temperature.The dried sample spot was then covered with a (1 µL) matrix of α-cyanohydroxy cinnamic acid (CHCA) to enable the proteins in the sample to crystallize.The MALDI bio target plate was then put into the MALDI-TOF apparatus.The identification score (from 0 to 3) was then used to characterize the amount of mass spectral concordance with the database.The MBT Compass and Flex Analysis tools were used to analyze and process these data.

Extraction of bioactive metabolites
The bacterial isolates No. RQ13 and RQ22 were grown on rice medium (100 g rice in 100 mL distilled water) and rice and yeast medium (100 g rice, 0.5 g yeast extract, in 100 mL distilled water).The rice mediums were incubated at 35 °C in static for 7 days.Simultaneously, the bacterial isolates No. RQ13 and RQ22 were cultured in tryptic soy broth and incubated at 35 °C with shaking at 120 rpm for 3 days 80 .After incubation, the broth media were centrifuged at 10,000 rpm (Thermo Fisher Scientific, USA) for 10 min at 4 °C to collect the CFS, which was then filtered through sterilized 0.22 µm pore-size filters (Millex-GS, Millipore, USA).Ethyl acetate was added to the CFS and rice medium in a 1:1 (v/v) ratio and vigorously agitated for a few minutes.The ethyl acetate mixtures were put into separating funnels and let to stand until the organic and aqueous phases separated, at which point the organic phase was collected and passed through anhydrous sodium sulfate.This procedure was performed three times before the organic phase was dried off using a rotary evaporator (Heidolph Instruments GmbH & Co. KG, Germany) to produce extracts 44 .

Determination of antifungal activity of bioactive metabolites
The antifungal potential of the extracts was assessed using an agar well diffusion experiment, as reported by Salman et al. 81 .On Petri dishes, potato dextrose agar medium was applied, and various fungal isolates (100 µL, 10 6 spores/mL) were dispersed equally across the agar surface with a sterile cotton swab, followed by wells cut with a sterile cork borer.Then, 100 µL of extracts No. 4 and 5 were applied to each well at a 5 mg/mL concentration.The Petri plates were incubated for 48 h at 28 °C, and the inhibition zones (mm) were measured to assess the antifungal activity.

Determination of volatile organic compounds in bioactive metabolites
The gas chromatography/mass spectrometer (GC/MS) technology (Agilent Technologies, USA) was used to undertake a qualitative and quantitative analysis of volatile organic molecules.A gas chromatograph (7890B) and a mass spectrometer detector (5977A) were part of the GC/MS system.The GC was outfitted with an HP-5MS column (30 m × 0.25 mm internal diameter and 0.25 m film thickness).The carrier gas in the analyses was hydrogen, with a flow rate of 1 mL/min at a splitless injection volume of 1 µL and the following temperature program: 50 °C for 1 min; 5 °C/min rise to 100 °C and hold for 0 min; 10 °C/min rise to 300 °C and hold for 5 min.The injector and detector were held at temperatures of 250 °C and 260 °C, respectively.With a 6-min solvent delay, electron ionization (EI) at 70 eV produced mass spectra with a spectral range of m/z 50

Determination of polyphenols in bioactive metabolites
Extracts were analyzed to assess polyphenols using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS), with an Exion LC AC system for separation and a SCIEX Triple Quad 5500 + MS/MS system with electrospray ionization (ESI) for detection.A ZORBAX SB-C18 Column (4.6 X 100 mm, 1.8 µm) (Agilent Technologies, USA) was employed for the separation.Two eluents were used in the mobile phases: A (0.1% formic acid in water) and B (acetonitrile).The mobile phase was set at 2% B from 0 to 1 min, 2% B from 1 to 21 min, 60% B from 21 to 25 min, and 2% B from 25 to 28 min.The injection volume was 3 µL, and the flow rate was 0.8 µL/min.The following parameters were employed for MRM analysis of the chosen polyphenols in both positive and negative ionization modes: Ion spray voltages for the positive and negative modes were 4500 and -4500, respectively; 400 °C source temperature; 25 psi curtain gas; 55 psi ion source gases with a declustering potential of 50; 25 psi collision energy; and 10 psi collision energy spread.

Evaluation of the effect of the bioactive metabolites on the microstructure of Aspergillus flavus using a SEM
The effect of extracts on A. flavus microstructure was investigated.Twenty-five milliliters of molten potato dextrose agar were put in Petri plates and permitted to solidify.A fungal spore suspension of A. flavus (100 µL, 10 6 spores/mL) was distributed evenly over the agar surface, after which wells were cut using a sterile cork borer.Each well received 100 µL of extracts Nos. 4 and 5, and the plates were incubated at 28 °C for 5 days.Mycelium segments (1 cm 2 ) were cut and deposited at room temperature in vials containing 3% glutaraldehyde in 0.05 M phosphate buffer (pH 6.8), as stated by Mims 82 and Gong et al. 83 .An ethanol series was used after chemical fixation, culminating in total ethanol.Fungal cultures were freeze-dried after samples were dried in liquid carbon dioxide.The samples were put in Petri plates, and an unfilled portion of the plate was filled with a vial cap holding 4% osmium tetraoxide in water.Then, segments were coated with 20 to 30 nm of 60:40 gold palladium.All materials were examined in a 20.00 kV electron probe micro-analyzer SEM (Quanta FEG 205, FEI Company, Hillsboro, OR, USA).

Effect of bioactive metabolites on fungal growth and aflatoxin production
The impact of extracts No. 4 and 5 on mycelial dry weight (MDW) and AFs production was determined using the method described by Roshan et al. 5 with a few adjustments (using potato dextrose broth instead of sucrose malt-yeast extract-broth).The appropriate amounts of extracts were added to reach final concentrations of 1, 3, 5, 7, and 9 mg/mL of growth media to various flasks containing 20 mL of potato dextrose broth.Each flask was filled with a fungal spore solution (100 µL, 10 6 spores/mL) from a 7-day-old culture of the aflatoxigenic isolate.For 10 days, cultures were incubated at 28 °C.After incubation, the culture medium was filtered (Whatman No. 1), and the mycelia were washed with water and dried in a hot air oven (110 °C, 12 h).In a separating funnel, the filtrate was extracted twice with 20 mL chloroform, and then the extract was passed through anhydrous sodium sulfate and evaporated to dryness.HPLC was used to identify aflatoxins.The percentage of inhibition was calculated using the following equation:

Brine shrimp lethality bioassay
The in vivo mortality of extracts No. 4 and 5 were estimated using nauplii of the A. salina.Twenty-seven g of the commercially available salt was dissolved with 900 mL of distilled water to make artificial saltwater.The A. salina eggs were placed in a small commercial tank with artificial seawater for nauplii hatching and incubated for 48 h under a halogen lamp, which provided direct light and warmth.Twenty mg of extracts No. 4 and 5 were diluted in 2 mL of ethyl acetate, and then concentrations of 50, 100, 200, 400, 600, 800, and 1000 g/mL were made.The tubes were allowed to dry out completely.Following that, each tube received 4.5 mL of artificial seawater, and ten nauplii were counted macroscopically and transferred to test tubes using the stem of a graduated Pasteur pipette against an illuminated backdrop.With artificial seawater, the final volume in each tube was adjusted to 5 mL after introducing the nauplii.Two separate counters counted and recorded the quantity of surviving nauplii in each tube after 24 h 84,85 .The experiment included three replicates for each treatment and 10 nauplii per replication.The LC 50 values were calculated with 95% confidence intervals using data analysis and interpreted using the Reed-Muench technique.The Reed-Muench technique presupposes that an animal that survives a particular dose will likewise survive any lower dose and that an animal that dies at a specific dose would similarly die with any higher dose.Thus, throughout the range of doses investigated, information from any group may add to knowledge from other groups 86,87 .

Cytotoxicity of human cell line
The impact of extracts No. 4 and 5 on HepG2 was investigated.At 37 °C and 5% CO 2 , cells were suspended in DMEM-F12 media supplemented with 1% antibiotic-antimycotic combination (10,000 U/mL potassium penicillin, 10,000 g/mL streptomycin sulfate, and 25 g/mL amphotericin B) and 1% L-glutamine.
Cell viability was determined using the mitochondrial-dependent reduction of yellow MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) to purple formazan 88 .Cells were cultivated for 10 days before www.nature.com/scientificreports/being seeded at a density of 10 × 10 3 cells/well in fresh complete growth medium on 96-well microtiter plates at 37 °C for 24 h in a water-jacketed carbon dioxide incubator (Sheldon, OR 97113, USA).The cells were cultivated alone (control) or with different extract concentrations to obtain a final concentration of (0.78, 1.56, 3.125, 6.25, 12.50, 25.00, 50.00, and 100.00 µg/mL).After 48 h, the medium was sucked; 40ul MTT salt (2.5 µg/mL) was added to each well and incubated for another four hours at 37 °C with 5% CO 2 .Each well received 200 µL of deionized water containing 10% sodium dodecyl sulfate (SDS) and was incubated overnight at 37 °C to terminate the reaction and dissolve the generated crystals.A positive control of Adriamycin (Doxorubicin), a recognized cytotoxic natural chemical with a 100% death rate under identical circumstances, was used at a 100 µg/mL concentration.
Using a microplate multi-well reader (Bio-Rad Laboratories Inc., model 3350, Hercules, California, USA), absorbance was measured at 595 nm and a reference wavelength of 620 nm.The extracts were dissolved in DMSO, with a final concentration of less than 0.2% on the cells.The following equation was used to compute the percentage of viability: The degree of selectivity of the synthesized compounds is stated in the current study as SI = IC 50 of the pure compound in a normal cell line/IC 50 of the same pure compound in a cancer cell line, where IC 50 is the concentration necessary to kill 50% of the cell population.In vitro, bioassay on human tumor cell line test was conducted by the Bioassay-cell culture Laboratory, National Research Centre, Cairo, Egypt.

Statistical analysis
The statistical analyses were conducted using the SPSS 26 (IBM, USA) software.The studies were carried out in triplicate, and the differences between control and treatment groups were assessed using the Student's t-test, while the differences across the groups were examined using the one-way ANOVA test.The significance threshold was chosen at P ≤ 0.05.

Conclusion
The isolated and identified Bacillus species showed variable degrees of antifungal activity.The bioactive metabolites extracted from these Bacillus species produced volatile organic compounds and polyphenols and exhibited antifungal and antiaflatoxigenic activity.These bioactive metabolites induced toxicity against A. salina and against hepatocellular carcinoma.This study is considered the first to report Bacillus bioactive metabolites' ability to reduce and prevent aflatoxin production.
MS result scores of the bacterial isolates showing antifungal activity, whereas the bacterial isolates No. RQ1, RQ5, RQ8, RQ13, and RQ16 were identified as Bacillus cereus DSM 31T DSM, with NCBI identifier 1396.The bacterial isolates No. RQ2, RQ7, and RQ15 were identified as Bacillus cereus with NCBI identifier 1396.On the other hand, the bacterial isolates RQ14 and RQ22 were identified as Bacillus thuringiensis DSM 2046T DSM with NCBI identifier 1428.The bacterial isolates No. RQ13 and RQ22 showing high antifungal activity were selected for the extraction of bioactive metabolites.A flow chart explaining the selection of bacterial isolates is shown in Fig. 1.Bioactive secondary metabolites were extracted from Bacillus thuringiensis (No.RQ22) (extracts No.

Figure 2 .
Figure 2. Flow chart showing the selection of suitable extracts that showed high antifungal activity.

Figure 3 .
Figure 3. Scanning electron microscope of (A) untreated A. flavus (control) showing typical conidia and conidiospores; (B) A. flavus after treatment with extract No. 4 (extracted from Bacillus cereus grown on tryptic soy broth) showing loss and mutation of fungal conidiospores; and (C) A. flavus after treatment with extract No. 5 (extracted from Bacillus cereus grown on rice medium) showing loss and mutation of fungal conidiospores.

Table 2 .
Biochemical characteristics and MALDI-TOF MS result scores of bacterial isolates showing antifungal activity.Range 2.00-3.00:High confidence and secure Genus and species Identification.Range 1.70-1.99:Secure Genus Identification with low-confidence species identification.Range 0.00 -1.69:Not reliable identification., 2, and 3) and from Bacillus cereus (No.RQ13) (extracts No. 4, 5, and 6).A flow chart explaining the selection of extracts is shown in Fig. 2.

Table 3 .
AntifungalData in Table3clearly showed that extracts No. 2 and 5 of bacteria grown on rice medium showed higher antifungal activity against A. flavus, A. niger, and Penicillium spp.On the other hand, extracts No. 1 and 4 of bacteria grown on tryptic soy broth showed antifungal activity against A. flavus and A. ochraceus.Results showed that extracts No. 3 and 6 of bacteria grown on rice yeast extract medium showed low antifungal activity.

Table 4 .
Volatile organic compounds of extract No. 4 RT, Retention time.a Anticancer; b Antioxidant; the activity of the chemical compounds is obtained from the National Center for Biotechnology Information.

Table 5 .
Volatile organic compounds of extract No. 5 RT, Retention time.The activity of the chemical compounds is obtained from the National Center for Biotechnology Information.a Antiviral.

Table 6 .
Contents of phenolic acids and flavonoids detected in bioactive metabolites extracted from Bacillus spp.The activity of the chemical compounds is obtained from the National Center for Biotechnology Information.RT, Retention time.a Antioxidant; b Anticancer; c Antiviral; d Antibacterial.

Table 7 .
43fect of bioactive metabolites extracted from Bacillus spp. on A. flavus growth and aflatoxin production.Values of dry mycelium weight were obtained by weighing mycelium mats.*Percentage of inhibition.total of 74 potential VOCs were identified43.Similar observations were reported by Rajaofera et al.
Figure 4. Effects of bioactive metabolites on A. salina mortality.Vol.:(0123456789)Scientific Reports | (2024) 14:16590 | https://doi.org/10.1038/s41598-024-66700-ywww.nature.com/scientificreports/ 44, who identified nineteen different VOCs from B. atrophaeus HAB-5.In a similar study, twenty-nine VOCs were identified from B. methylotrophicus BCN2.Meanwhile, thirty VOCS were identified from B. thuringiensis BCN10 63ported similar results and found that Bacillus extract inhibited the Effect of different concentrations of extract No. 5 on HepG2 cell line viability.growth of Candida albicans and Aspergillus niger.Miljaković et al.62reported similar observations, stating that B. cereus MH778713's antifungal activity could be linked to the generation of diffusible metabolites and hydrolyzing enzymes.Although only one Bacillus extract had antifungal activity on F. oxysporum, Ramírez et al.63revealed that B. cereus MH778713 VOCs reduced the mycelial radial growth of F. oxysporum by 38%.
-550.Different components were found by comparing the spectrum fragmentation pattern to those in the Wiley and NIST Mass Spectral Library data.